Jagua Ink
⚠️ Moderate Risk
FEI: 3008780155 • Plaza Panama, Provincia de Panama • PANAMA
FEI Number
3008780155
Location
Plaza Panama, Provincia de Panama
Country
PANAMAAddress
Calle 50 Final Con 76 Edificio, , Plaza Panama, Provincia de Panama, Panama
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
Refusal History
Frequently Asked Questions
What is Jagua Ink's FDA import refusal history?
Jagua Ink (FEI: 3008780155) has 2 FDA import refusal record(s) in our database, spanning from 3/23/2011 to 3/23/2011.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Jagua Ink's FEI number is 3008780155.
What types of violations has Jagua Ink received?
Jagua Ink has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Jagua Ink come from?
All FDA import refusal data for Jagua Ink is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.